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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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ATTUNE KNEE SYSTEM REVISION TIBIAL AUGMENT UNIVERSAL 5MM CEMENTED SIZE 1/2
DEPUY (IRELAND)
1523-01-001
In Commercial Distribution

  • 10603295057499 ()
152301001

  • Knee arthroplasty wedge
No Description
Zimmer, Inc.
5880-06-10
In Commercial Distribution

  • 00889024199071 ()

  • Size 6, 10 mm, Thickness
00-5880-006-10

  • Knee arthroplasty wedge
No Description
Zimmer, Inc.
5880-05-10
In Commercial Distribution

  • 00889024199057 ()

  • Size 5, 10 mm, Thickness
00-5880-005-10

  • Knee arthroplasty wedge
No Description
Zimmer, Inc.
5880-04-10
In Commercial Distribution

  • 00889024199033 ()

  • Size 4, 10 mm, Thickness
00-5880-004-10

  • Knee arthroplasty wedge
No Description
Zimmer, Inc.
5880-03-10
In Commercial Distribution

  • 00889024199019 ()

  • Size 3, 10 mm, Thickness
00-5880-003-10

  • Knee arthroplasty wedge
No Description
Zimmer, Inc.
5880-02-10
In Commercial Distribution

  • 00889024198982 ()

  • Size 2, 10 mm, Thickness
00-5880-002-10

  • Knee arthroplasty wedge
No Description
Zimmer, Inc.
5880-01-10
In Commercial Distribution

  • 00889024198951 ()

  • Size 1, 10 mm, Thickness
00-5880-001-10

  • Knee arthroplasty wedge
No Description
Zimmer, Inc.
6215-04-400
In Commercial Distribution

  • 00889024252172 ()

  • Size 4, 4mm
6215-04-400

  • Knee arthroplasty wedge
No Description
Zimmer, Inc.
6215-04-301
In Commercial Distribution

  • 00889024252165 ()

  • Size 3, 4mm
6215-04-301

  • Knee arthroplasty wedge
No Description
Zimmer, Inc.
6215-04-300
In Commercial Distribution

  • 00889024252158 ()

  • Size 3, 4mm
6215-04-300

  • Knee arthroplasty wedge
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